PMID- 7989932 OWN - NLM STAT- MEDLINE DCOM- 19950112 LR - 20170210 IS - 0732-183X (Print) IS - 0732-183X (Linking) VI - 12 IP - 12 DP - 1994 Dec TI - Allogeneic bone marrow transplantation in adult acute lymphoblastic leukemia in first complete remission: a comparative study. French Group of Therapy of Adult Acute Lymphoblastic Leukemia. PG - 2580-7 AB - PURPOSE: Optimal postremission therapy remains controversial in adult patients with acute lymphoblastic leukemia (ALL). In a large multicentric trial (LALA87), we compared allogeneic bone marrow transplantation (BMT) with other postremission therapies (chemotherapy or autologous transplantation) using the result of the human leukocyte antigen (HLA) typing as a random allocation. PATIENTS AND METHODS: Patient eligibility requirements were as follows: (1) inclusion in LALA87 trial, (2) complete response to induction or salvage therapy, (3) age 15 to 40 years, and (4) at least one potential sibling donor. Patients with an HLA-identical sibling were assigned to the BMT group, while patients without a sibling donor constituted the control group. Allogeneic transplantation was scheduled for patients in the BMT group; in the control group, patients were randomly allocated to receive chemotherapy or autologous transplantation. RESULTS: Of 284 eligible points, 257 entered the study: 116 were allocated to the BMT group and 141 to the control group. The 5-year survival rates were not statistically significantly different between the two groups. When only patients with high-risk ALL were considered (those with [1] Philadelphia chromosome [Ph1] ALL, [2] null or undifferentiated ALL, or [3] c-ALL with either age greater than 35 years or WBC count > 30 x 10(9)/L or time to achieve complete remission > 4 weeks), overall survival (P = .03) and disease-free-survival (P = .01) were better for the BMT group compared with the control group (5-year overall survival rates, 44% v 20%; 5-year disease-free survival rates, 39% v 14%). CONCLUSION: Allogeneic transplantation does not improve survival in patients with standard-risk ALL and should be recommended only for patients with adverse prognostic factors. FAU - Sebban, C AU - Sebban C AD - Department of Hematology, Hopital Edouard Herriot, Lyon, France. FAU - Lepage, E AU - Lepage E FAU - Vernant, J P AU - Vernant JP FAU - Gluckman, E AU - Gluckman E FAU - Attal, M AU - Attal M FAU - Reiffers, J AU - Reiffers J FAU - Sutton, L AU - Sutton L FAU - Racadot, E AU - Racadot E FAU - Michallet, M AU - Michallet M FAU - Maraninchi, D AU - Maraninchi D AU - et al. LA - eng PT - Clinical Trial PT - Comparative Study PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, Non-U.S. Gov't PL - United States TA - J Clin Oncol JT - Journal of clinical oncology : official journal of the American Society of Clinical Oncology JID - 8309333 RN - 5J49Q6B70F (Vincristine) RN - 8N3DW7272P (Cyclophosphamide) RN - VB0R961HZT (Prednisone) RN - COP protocol 2 SB - IM MH - Adolescent MH - Adult MH - Antineoplastic Combined Chemotherapy Protocols/*therapeutic use MH - *Bone Marrow Transplantation MH - Cyclophosphamide/administration & dosage MH - Female MH - Histocompatibility Testing MH - Humans MH - Male MH - Precursor Cell Lymphoblastic Leukemia-Lymphoma/mortality/*therapy MH - Prednisone/administration & dosage MH - Prognosis MH - Remission Induction MH - Survival Rate MH - Transplantation, Autologous MH - Transplantation, Homologous MH - Vincristine/administration & dosage EDAT- 1994/12/01 00:00 MHDA- 1994/12/01 00:01 CRDT- 1994/12/01 00:00 PHST- 1994/12/01 00:00 [pubmed] PHST- 1994/12/01 00:01 [medline] PHST- 1994/12/01 00:00 [entrez] AID - 10.1200/JCO.1994.12.12.2580 [doi] PST - ppublish SO - J Clin Oncol. 1994 Dec;12(12):2580-7. doi: 10.1200/JCO.1994.12.12.2580.